Save up -80% on Conivaptan

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RX BIN: 015558RX PCN: HTGroup ID: DDN6600Card Holder ID: DDN6600
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2019 Price of Conivaptan

Vaprisol 20 mg/100 ml bag

$6.3ml
price without discount in nearest pharmacy. Price may vary.

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We offer free Conivaptan coupons and discounts that may help you save up to 80% off the retail price in your local pharmacy. Just print your coupon! It’s ready to use and never expire. Present your discount card in most local pharmacies to get a discount on Conivaptan every time. What are you waiting for? Claim your prescription drug card now!

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2018 Statistics

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Discount Cards 16,000+

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Clients Benefit 29%

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Total savings $4,735,080

What is Conivaptan

Conivaptan is a non-peptide inhibitor of antidiuretic hormone (vasopressin). It was approved in 2004 for hyponatremia (low blood sodium levels) caused by syndrome of inappropriate antidiuretic hormone (SIADH). Conivaptan inhibits both isotypes of the vasopressin receptor (V1a and V2).

Conivaptan mechanism of action

Conivaptan is a dual AVP antagonist with nanomolar affinity for human arginine vasopressin Vsub1A/sub and Vsub2/sub receptors iin vitro/i. This antagonism occurs in the renal collecting ducts, resulting in aquaresis, or excretion of free water.

Dosage forms of Conivaptan

FormRouteStrength
Injection, solutionintravenous20 mg/100mL

Prescription Generics

false

International Brands

Vaprisol Dextrose In Plastic Container

Synonyms

4′-((4,5-dihydro-2-Methylimidazo(4,5-D)(1)benzazepin-6(1H)-yl)carbonyl)-2-biphenylcarboxanilide Conivaptan

Manufacturers

Cumberland Pharmaceuticals Inc.

CAS number

210101-16-9

UNII

0NJ98Y462X

State

solid

Affected organisms

Humans and other mammals

Indication of Conivaptan

For the treatment of euvolemic or hypervolemic hyponatremia (e.g. the syndrome of inappropriate secretion of antidiuretic hormone, or in the setting of hypothyroidism, adrenal insufficiency, pulmonary disorders, etc.) in hospitalized patients.

Toxicity of Conivaptan

Although no data on overdosage in humans are available, conivaptan has been administered as a 20 mg loading dose on Day 1 followed by continuous infusion of 80 mg/day for 4 days in hyponatremia patients and up to 120 mg/day for 2 days in CHF patients. No new toxicities were identified at these higher doses, but adverse events related to the pharmacologic activity of conivaptan, e.g. hypotension and thirst, occurred more frequently at these higher doses.

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